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Harnessing CRISPR-Cas system diversity for gene editing technologies

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The discovery and utilization of RNA-guided surveillance complexes,such as CRISPR-Cas9,for sequence-specific DNA or RNA cleavage,has revolutionised the process of gene modification or knockdown.To optimise the use of this technology,an exploratory race has ensued to discover or develop new RNA-guided endonucleases with the most flexible sequence targeting requirements,coupled with high cleavage efficacy and specificity.Here we review the constraints of existing gene editing and assess the merits of exploiting the diversity of CRISPR-Cas effectors as a methodology for surmounting these limitations.

Alexander McKay、Gaetan Burgio

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Department of Immunology and Infectious Diseases, John Curtin School of Medical Research, Australian National University, Canberra, ACT 2601, Australia

Gaetan Burgio is supported by the National Collaborative Research Infrastructure(NCRIS) via Phenomics AustraliaNational Health and Medical Research Council of AustraliaAustralian Research CouncilNational Natural Science Foundation of China

APP1143008DP18010149481772214

2021

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生物医学研究杂志(英文版)
南京医科大学

生物医学研究杂志(英文版)

CSCD
影响因子:0.794
ISSN:1674-8301
年,卷(期):2021.35(2)
Alexander McKay,Gaetan Burgio.Harnessing CRISPR-Cas system diversity for gene editing technologies[J].生物医学研究杂志(英文版),2021,35(2):91-106.
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